Details
Originalsprache | Englisch |
---|---|
Seiten (von - bis) | 696-699 |
Seitenumfang | 4 |
Fachzeitschrift | Organic Letters |
Jahrgang | 14 |
Ausgabenummer | 3 |
Publikationsstatus | Veröffentlicht - 19 Jan. 2012 |
Abstract
A total synthesis of millingtonine A, a diglycosylated alkaloid, has been accomplished. Millingtonine A possesses a unique racemic tricyclic core structure not known from any other natural or synthetic source until now. The synthesis features a key bond-forming radical Ueno - Stork cyclization to form the heterocyclic core.
ASJC Scopus Sachgebiete
- Biochemie, Genetik und Molekularbiologie (insg.)
- Biochemie
- Chemie (insg.)
- Physikalische und Theoretische Chemie
- Chemie (insg.)
- Organische Chemie
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in: Organic Letters, Jahrgang 14, Nr. 3, 19.01.2012, S. 696-699.
Publikation: Beitrag in Fachzeitschrift › Artikel › Forschung › Peer-Review
}
TY - JOUR
T1 - A total synthesis of millingtonine a
AU - Wegner, Jens
AU - Ley, Steven V.
AU - Kirschning, Andreas
AU - Hansen, Anne Lene
AU - Montenegro Garcia, Javier
AU - Baxendale, Ian R.
PY - 2012/1/19
Y1 - 2012/1/19
N2 - A total synthesis of millingtonine A, a diglycosylated alkaloid, has been accomplished. Millingtonine A possesses a unique racemic tricyclic core structure not known from any other natural or synthetic source until now. The synthesis features a key bond-forming radical Ueno - Stork cyclization to form the heterocyclic core.
AB - A total synthesis of millingtonine A, a diglycosylated alkaloid, has been accomplished. Millingtonine A possesses a unique racemic tricyclic core structure not known from any other natural or synthetic source until now. The synthesis features a key bond-forming radical Ueno - Stork cyclization to form the heterocyclic core.
UR - http://www.scopus.com/inward/record.url?scp=84856753223&partnerID=8YFLogxK
U2 - 10.1021/ol203158p
DO - 10.1021/ol203158p
M3 - Article
C2 - 22260734
AN - SCOPUS:84856753223
VL - 14
SP - 696
EP - 699
JO - Organic Letters
JF - Organic Letters
SN - 1523-7060
IS - 3
ER -